Duns Number:276816717
Device Description: The VIDAS ® Creatine Kinase MB (CKMB) Assay is intended for use on the VIDAS instruments f The VIDAS ® Creatine Kinase MB (CKMB) Assay is intended for use on the VIDAS instruments for the determination of creatine kinase MB isoenzyme concentration in serum or plasma.
Catalog Number
-
Brand Name
VIDAS® CK-MB
Version/Model Number
30421-01
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
January 01, 2018
Issuing Agency
In GS1
MRI safety Status
Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)
-
Device labeled as "Not made with natural rubber latex"
-
For Single-Use
-
Prescription Use (Rx)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
JHX
Product Code Name
Fluorometric Method, Cpk Or Isoenzymes
Public Device Record Key
3f0217f8-2f04-4a44-9af7-579fd2eca177
Public Version Date
May 14, 2020
Public Version Number
4
DI Record Publish Date
August 31, 2016
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 82 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 156 |
| 3 | A medical device with high risk that requires premarket approval | 3 |